Viewing Study NCT06498557



Ignite Creation Date: 2024-07-17 @ 10:58 AM
Last Modification Date: 2024-10-26 @ 3:34 PM
Study NCT ID: NCT06498557
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-07-12
First Post: 2024-06-29

Brief Title: Postoperative Analgesis in Total Knee Arthroplasty
Sponsor: Samsun University
Organization: Samsun University

Study Overview

Official Title: Results of Postoperative Analgesis Protocols Applied in Total Knee ArthroplastyObservational Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Postoperative analgesic treatment methods are applied to patients who have undergone knee arthroplasty These applications are a routine part of the procedure It is medically and ethically necessary Postoperative analgesia applications are started during the intraoperative period and continued during the postoperative period The analgesia protocol to be used is shaped by the characteristics of the patient and the skill and experience of the anesthesiologist The scientifically accepted method is multimodel analgesia protocols These protocols cover a wide range from paracetamol to opioids to peripheral and central blocks methods such as suprainguinal fascia iliac block SFIP adductor block ACB and infiltration analgesia IPACK applied between the posterior elements of the knee and the popliteal artery Our aim in this study is to evaluate the effects of analgesia protocols applied to patients undergoing knee arthroplasty surgery on inflammatory biomarkers such as neutrophil lymphocyte ratio NLR platelet lymphocyte ratio PLR systemic immune inflammation score SII lactate obtained from routine blood and blood gas examinations in the first 24 hours of the postoperative period
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None